The Potential of Medicinal Plants and Natural Products in the Treatment of Burns and Sunburn—A Review
Abstract
:1. Introduction
2. Materials and Methods
3. Results
3.1. Clinical Trials—Single Preparations
3.1.1. Albizia julibrissin
3.1.2. Aloe vera
3.1.3. Arnebia euchroma
3.1.4. Betula pendula, Betula pubescens
3.1.5. Camellia sinensis
3.1.6. Centella asiatica
3.1.7. Hippophaë rhamnoides
3.1.8. Juglans regia
3.2. Clinical Trials—Mixtures of Natural Products
3.2.1. Alkanna tinctoria, Olive Oil, and Beeswax
3.2.2. Aloe vera and Centella asiatica
3.2.3. Aloe vera, Lavandula stoechas, and Pelargonium roseum
3.2.4. Azadirachta indica Oil and Hypericum perforatum Oil
3.2.5. Lawsonia inermis and Beeswax
3.2.6. Matricaria chamomilla, Rosa canina and Beeswax
3.3. In Vivo Studies on Animal Models of Burn
4. Discussion
5. Conclusions
Supplementary Materials
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
References
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Plant Material | Animal Model | Burn Wound | Treatment Schedule and Study Groups * | Results | Ref. |
---|---|---|---|---|---|
Aegialitis rotundifolia leaves ethanolic extract | Wistar albino rats, male | Chemical burn—a few drops of concentrated hydrochloric acid Thermal burn—metal rod heated over the open flame for 30 s | Once a day for 18 days E: 2.5% and 5% (w/w) in the simple ointment S: 1% SSD cream C: simple ointment | The experimental and standard groups significantly increased the percentage of wound closure and decreased epithelisation time after chemical and thermal burns compared to the control group. | [39] |
Achillea millefolium aerial parts ethanolic extract | New Zealand white rabbits, male | Third-degree thermal burn—heated metal plate (170 °C) applied for 10 s | Once a day for 21 days E: 5 mL of extract C: 5 mL of normal saline | From the 7th day of treatment, the wound area in the experimental group was significantly smaller than in the control group. After histopathological analysis in the experimental group, complete filling with granulation tissue, an increased amount of collagen fibres and a decrease in the number of inflammatory cells were observed, while in the control group, only fresh granulation tissue was observed. The number of isolated microorganisms decreased in the experimental group. | [40] |
Achyranthes aspera leaves methanolic extract | Albino rats, either sex | Third-degree thermal burn—metal rod heated to 85 °C, pressed for 20 s | Twice a day for 7 days E: 5.0% (w/w) of extract in soft white petroleum S: Himax® (traditional Ayurvedic ointment) C: soft white petroleum | On the 8th day, the wound area of the experimental group was significantly smaller than that of the control and standard groups. From the biochemical parameters, a higher content of protein, vitamin C, glutathione, catalase, superoxide dismutase, and hydroxyproline were noted in the experimental group than in the control and standard group. The concentration of matrix metalloproteinase 9 and matrix metalloproteinase 2 was higher in the experimental than in the control group. Moreover, there were more collagen fibres, and the proliferation of fibroblasts increased. | [41] |
Actinida deliciosa fruits freshly sliced | Wistar albino rats, male | Second-degree thermal burn—hot plate warmed up to 110 °C, placed for 10 s | Once a day for 21 days E: sliced fresh kiwifruit (3 mm thick) S: 1% SSD cream C: Vaseline | The wound area in the experimental group was significantly smaller, and complete wound closure was observed faster than in the standard and control groups. In the macroscopic evaluation, in the experimental group, compared to other groups, an increase in hyperaemia was observed in the first days, and after 11 days, a significant decrease, moreover after 5 days, a reduction in oedema, as well as earlier epithelisation. Histopathological analysis showed significantly less inflammation and a higher score of vascularisation than the other groups, as well as a score of granulation similar to the standard group. Fewer bacteria were isolated from the wound of the experimental group. It has been shown that applying kiwi to a wound results in its enzymatic debridement. | [42] |
Actinida deliciosa fruits freshly cut kiwifruit mixed with kiwi juice | Sprague-Dawley rats, male | Third-degree thermal burn—copper stamp, kept at 90 °C for 15 min | Once a day for 30 days E: freshly cut kiwifruit mixed with kiwi juice C: neutral ointment | After 20 days, the eschar separation was significantly accelerated in the experimental group. In addition, a significantly reduced wound surface area and better wound closure were observed than in the control group. No differences were observed in the microscopic assessment of the degree of vascularisation, collagen precipitation and acute and chronic inflammation level. | [43] |
Allium cepa bulbs poultice | Holtzman albino rats, male | Second-degree thermal burn—hot 60-watt bulb, applied 3 times for 20 s | Once a day for 21 days E: 4 g of poultice S: 1% SSD cream C: w/o treatment | The wound area after 21 days in the experimental and control groups was similar and significantly smaller than in the control group. In the experimental group, the histopathological examination showed the presence of skin composed of a reticular stratum of fibroblasts, collagen, and several blood vessels. In contrast, only fibroblasts and collagen were present in the standard group; in the control group, a hyperaemic chorion was. | [44] |
Aloe vera fresh leaves dry powder of leaf gel | Wistar albino rats, male | Second-degree thermal burn—hot water (90 °C), applied for 6 s | Twice a day for 25 days E: 0.5% of Aloe gel powder in base cream S: 1% SSD cream C: base cream N: w/o treatment | After 25 days, the mean wound size was 0.78 ± 1.3, 4.1 ± 3.6, 4 ± 2.3, and 5.5 ± 3 for the experimental, standard, control, and negative control groups, respectively, and was significantly lowest in the experimental group. The biopsy showed that epidermal re-epithelialisation and skin fibrosis were observed in the experimental group. Inflammation and granulation tissue were minimal, and no bacteria were found. Wound healing was significant in this group compared to the standard group. In the control groups, healing was minimal or negligible, and bacteria were present in the wounds. | [45] |
Aloe vera fresh leaves dry powder of leaf juice | Wistar albino rats, female | Second-degree thermal burn—a piece of the aluminium heated to 100 °C, applied for 15 s | Once a day for 30 days E: 1 mL of 2% Aloe gel NC: w/o treatment | After 24 days, significant differences in the degree of wound closure and epithelialisation were observed between the groups. In the experimental group, wound closure was 95.64 ± 1.99%, and the time of complete epithelisation was 27 days, while in the control group, it was 80.15 ± 2.80% and 32.5 days, respectively. Histopathological analysis showed that after 18 days of treatment in the experimental group, the number of inflammatory cells was significantly lower, and the degree of epithelialisation and neo-angiogenesis was significantly higher compared to the control group. | [46] |
Aloe vera leaves 30% (v/v) methanolic extract | Wistar albino rats, male | Second-degree thermal burn—metal plate heated in boiling water for 5 min, applied for 10 s | Twice a day for 21 days E: 0.5, 1, 1.5 or 2% of extract in Eucerin S: 1% SSD cream C: Eucerin N: w/o treatment | The degree of wound closure in the experimental groups was higher than in the control groups. After 21 days, the wound area of the group treated with 1.5 and 2% extract was smaller than in the standard group. Histopathological analysis showed better wound healing parameters for the experimental and standard groups than in the control group, such as the number of hair follicles, sebaceous glands, fibroblasts, macrophages, neutrophils, blood vessels, and the thickness of the epidermal layer. | [47] |
Anredera cordifolia leaves ethanolic extract | White rats (Rattus norvegicus), male | Thermal burn—iron plate soaking in boiling water for 5 min, applied for 30 s | Three times a day for 14 days E: 2.5, 5 or 7.5% of extract in Vaseline S: 1% SSD cream | Statistically, the best results were obtained in the experimental group treated with 5% of the extract. The highest degree of collagen deposition, the lowest infiltration of polymorphonuclear cells, mild angiogenesis, and moderate fibrosis were observed there. In the standard group, the degree of healing was the lowest. | [48] |
Arnebia euchroma whole plant 50% (v/v) ethanolic extract | Sprague-Dawley rats, female | Third-degree thermal burn—iron plate heated to 100 °C, applied for 40 s | Once a day for 17 days E: 10 or 20% of extract in a carboxymethylcellulose (CMC) gel C: CMC gel N: w/o treatment | The degree of wound closure after 18 days was significantly higher in the group treated with 20% of the extract. However, the histopathological analysis showed the highest content of fibroblasts, collagen, and blood vessels in both experimental groups. | [49] |
Arnebia euchroma leaves and root unspecified extract | Wistar albino rats, female | Second-degree thermal burn—aluminium plate heated to 60 °C, applied for 5 s | Once a day for 28 days E: 10 or 20% (v/v) of extract in vehicle gel S: 1% SSD cream N: w/o treatment | Compared to the control group, the treatment groups showed an increase in the amount of granulation tissue, degree of epithelisation, reduction of the wound area, fibroblast proliferation, volume of collagen fibres, and length and diameter of blood vessels. Wound closure was the fastest in the group treated with 10% extract, and fibroblast proliferation was the highest in the group treated with 20%. | [17] |
Azadirachta indica leaves 90% (v/v) ethanolic extract | Wistar albino rats, male | Second-degree thermal burn—hot wax (80 °C), applied until solidified | Once a day (0.5 g per wound) for 15 days E: 1% of extract in base gel S: 1% SSD cream C: base gel | The average wound closure after 15 days in the experimental group was 81.25 ± 0.7822%, and in the standard group, 90.43 ± 0.7691%, which were higher values than in the control group (68.58 ± 0.7791%). The average re-epithelialisation time was 28.77 ± 1.22 days in the experimental group and 25.20 ± 2.10 days in the standard group, while in the control group, it was significantly longer–38.36 ± 1.77 days. | [50] |
Bauhinia purpurea leaves methanolic extract | Sprague-Dawley rats | Second-degree thermal burn—hot molten wax (80 °C), applied until solidified | Once a day for 22 days E: 2.5 or 5% of extract in a simple ointment S: 5% of Aloe vera extract C: simple ointment | The wound epithelialisation period was 15.83 ± 0.30, 14.33 ± 0.49, 12.16 ± 0.40 and 13.13 ± 0.40 days for the control, treated with 2.5% extract, treated with 5% extract and standard groups, respectively. The period was statistically significantly shorter for the group treated with 5% extract and the standard group compared to the control. | [51] |
Bauhinia purpurea leaves chloroform extract | Sprague-Dawley rats | Second-degree thermal burn—hot molten wax (80 °C), applied until solidified | Once a day for 22 days E: 2.5 or 5% of extract in Carbopol base S: 5% of Aloe vera extract C: Carbopol base | The period of wound epithelialisation in the group treated with 5% of the extract and the standard group was 14.50 ± 0.42 and 13.13 ± 0.40 days, respectively, and was statistically significantly shorter than in the control group and the group treated with 2.5% extract, in which it was 16.50 ± 0.50 and 16.33 ± 0.49 days, respectively. | [51] |
Brassica oleracea leaves aqueous extract | Sprague-Dawley rats, female | Second-degree thermal burn—hot metal stamp (80 °C), applied for 10 s | Once a day for 28 days E: 1 g of extract per 1 mL base cream (70% sorbitol in glycerin) S: 1% SSD cream C: base cream NC: w/o treatment | Compared to other groups, the experimental group showed a decrease in the fibrinoleukocytic layer and an increase in granulation tissue, as well as a decrease in the number of macrophages and neutrophils in the experimental group at the end of the 2nd week. However, at the end of the 3rd week, the stratum keratinosum was formed, the number of fibroblasts and macrophages increased, and the number of neutrophils decreased. At the end of the 4th week, the epidermis was fully developed. | [52] |
Camelia sinensis leaves 70% (v/v) ethanolic extract | Wistar albino rats, male | Second-degree thermal burn—hot metal plate (120 °C), applied for 5 s | Once a day (1 g per wound) for 21 days E: 0.6% of extract in Vaseline C: Vaseline NC: normal saline | The average healing time was significantly shorter in the experimental group compared to the control group. In histopathological analysis, a significantly lower number of inflammatory cells was observed in the experimental group during the entire study, and no significant differences in epidermal regeneration and angiogenesis were observed. On the 21st day, angiogenesis was significantly higher, and there were no significant differences in other parameters. | [53] |
Camelia sinensis leaves 70% (v/v) ethanolic extract | Wistar albino rats, male | Second-degree thermal burn—metal cube heated to 100 °C, applied for 15 s | Once a day for 14 days E: 2% of extract in normal saline S: 1% SSD cream C: normal saline | The average burn area was significantly smaller in the experimental group compared to the negative control group. No significant differences in burn size, vascularisation, number of inflammatory cells, and epithelisation were observed between the experimental, standard, and control groups. | [54] |
Carissa spinarum roots methanolic extract | Swiss albino mice, either sex | Second-degree thermal burn—hot aluminium plate (85 °C), applied for 5 s | Once a day for 36 days E: 1 or 2.5% of extract in an ointment base S: 1% SSD cream C: ointment base NC: w/o treatment | From day 20, the experimental and standard groups observed a significant increase in wound closure. Reepithelialisation time was significantly reduced compared to controls in the group treated with 2.5% extract and 1% SSD cream. In the histological examination in the group treated with 2.5% of the extract compared to the other groups, healing was advanced. There was a complete renewal of the epidermis, an increase in the amount of collagen and a decrease in the number of inflammatory cells. In addition, the hydroxyproline content was significantly higher. | [55] |
Centella asiatica herb 70% (v/v) ethanolic extract | albino mice, male | Chemical burn—50% phenol solution, applied for 30 s | Once a day for 10 days E: 2% of extract in base gel S: Bioplacenton® jelly (neomycin + placenta extract) C: base gel | Treatment with C. asiatica gel improves wound healing compared to the control group but less than in the standard group. Complete wound closure in the experimental group was observed after 8 days, in the standard group after 6 days, while in the control group, after 10 days, the wound closure was only 75.34 ± 20.709%. | [56] |
Centella asiatica aerial parts n-hexane, ethyl acetate, methanolic and aqueous extracts | Sprague-Dawley rats, male | Second-degree thermal burn—hot plate heated to 75 °C, applied for 10 s | Once a day (0.5 mL per wound) for 14 days E: 10% of appropriate extract in vehicle C: vehicle or normal saline NC: w/o treatment | The degree of wound healing was statistically significantly higher in the experimental groups than in the control groups. After 14 days, it was 53.87 ± 4.64, 57.53 ± 5.68, 60.31 ± 5.70, and 59.82 ± 8.31% for the hexane, ethyl acetate, methanolic, and aqueous extracts, respectively, and 38.07 ± 5.15, 31.85 ± 2.66, and 25.36 ± 1.81% for the vehicle, normal saline, and untreated controls, respectively. In the histopathological analysis of the experimental groups, in contrast to the control groups, fully developed epithelisation and keratinisation were observed without necrosis and inflammation. | [57] |
Cleistocalyx operculatus leaves hydrodistillation | Swiss albino mice, male | Second-degree thermal burn—aluminium bar heated to 100 °C, applied for 15 s | Once a day (50 µL per wound) for 20 days E: 1% of essential oil (in 0.1% DMSO and Tween 20 solution) S: Tamanu oil C: normal saline | The wound area of the experimental group after 10 and 20 days was significantly smaller than in the control and standard groups. In the histopathological analysis in the experimental group, in contrast to the other groups, re-epithelialisation was completed. Fewer inflammatory cells, thick, neatly arranged fibres, and mature hair follicles were observed. | [58] |
Copaifera officinalis oleoresin | Swiss mice, male | UVB radiation-induced paw burn model (0.61 mW/cm2, 0.75 J/cm2) | Once a day (15 mg per paw) for 6 days E: 3% of oleoresin in base cream S: 1% SSD cream C: base cream NC: w/o treatment | Mechanical allodynia lasting 6 days in the untreated group was significantly reduced from the second day of treatment in the experimental group and the third day in the standard group. Irradiation-induced thermal hyperalgesia was abolished more strongly in the experimental group than in the other groups. Infiltration of inflammatory cells after irradiation was significantly reduced in the experimental and standard groups, while increased skin thickness was significantly reduced only in the standard group. | [59] |
Crocus sativus stigmas 70% (v/v) ethanolic extract | Sprague-Dawley rats, male | Third-degree thermal burn—aluminium bar boiled in water for 30 s, applied for 10 s | Once a day for 28 days E: 20% of extract in 1% SSD cream S: 1% SSD cream NC: w/o treatment | The percentage of wound closure was significantly higher in the experimental group after 7 days compared to the others. After 14 days, the wounds of the experimental and the standard groups were almost completely closed. In the experimental group, inflammation and redness were significantly reduced, and scarring was minimal. Histopathological analysis after 14 days showed an increase in the number of cells, blood vessels, fibroblasts, and fibrocytes in the experimental group compared to the standard, as well as a comparable, lower than in control, number of inflammatory cells. After 28 days, the number of inflammatory cells, fibrocytes, fibroblasts and total cells significantly decreased in the experimental group compared to the control. In addition, the secretion of interleukin 1β and tumour growth factor β1 was reduced, and the hydroxyproline content was increased. | [60] |
Cucurbita moschata fruit peel 70% (v/v) ethanolic extract | Wistar albino rats, male | Second-degree thermal burn—electrical heater (110 °C), applied for 10 s | Once a day for 14 days E: 10 or 20% of extract in Eucerin S: 1% SSD cream C: Eucerin | The degree of wound closure after 14 days was 57.80 ± 5.71, 78.80 ± 3.96, 77.60 ± 5.41, and 90.80 ± 5.86% for the group, standard, treated with 10% extract and treated with 20% extract groups, respectively. It was significantly lowest in the control group and significantly highest in the group treated with 20% of the extract. Tissue analysis of oxidative stress biomarkers showed that lipid peroxidation in the standard and experimental groups was significantly reduced compared to the control group. The total antioxidant power and total thiol molecules content were significantly higher in the standard group and the group treated with 20% extract than in the control group. In histopathological analysis, the group treated with 20% extract showed better signs of wound healing. Inflammatory cells were absent, collagen fibres were well organised, and the basal epithelial layer reached a normal level. | [61] |
Cucurbita moschata oil | BALB/c albino mice, male | Third-degree thermal burn—coin heated for 3 min with a spirit lamp, applied for 8 s | Once a day for 28 days E: 30 or 40% of oil NC: w/o treatment | Compared to the negative control, the group treated with sesame oil showed better wound healing, higher total antioxidant power, and lower malondialdehyde levels than the control. | [62] |
Ephedra alata whole plant 2-step extraction with n-hexane and 50% (v/v) ethanol | Syrian hamsters (Mesocricetus auratus), male | Third-degree thermal burn—metal plate boiled in water for 5 min | Once a day for 15 days E: 1.5% of extract in an ointment base C: ointment base NC: w/o treatment | In the macroscopic assessment, the burn wound of the experimental group healed faster and better than in the other groups. However, in the histopathological analysis, no statistically significant differences in the degree of fibrosis and collagen fibres density were observed compared to the control group. | [63] |
Globularia alypum leaves methanolic extract | Wistar albino rats, male | Second-degree thermal burn—electric heater (110 °C), applied for 10 s | Once a day for 16 days E: extract in glycerol (unspecified concentration) S: Cytol Centella® cream (with Centella asiatica) C: glycerol NC: normal saline | From day 12, the wound closure of the experimental group was significantly better compared to the untreated group. The hydroxyproline level in the experimental group was significantly higher than in the other groups. In the histopathological analysis after 16 days, the appearance of the epidermis and skin in the experimental group was normal, while in the standard group, there were signs of inflammation. In the untreated groups, there was a massive infiltration of inflammatory cells without a developed epidermal layer. | [64] |
Glycyrrhiza glabra roots 75% (v/v) ethanolic extract | Sprague-Dawley rats, male | Third-degree thermal burn—hot plate | Once a day for 29 days E: 10% of extract in base gel S: 1% SSD cream C: base gel NC: w/o treatment | After 14 days, no signs of wound closure were observed macroscopically in the experimental group. Histopathological evaluation of this group showed complete re-epithelialisation, minimal granulation tissue formation, mild inflammation, and irregular collagen distribution. In contrast, in the standard group, only granulation tissue and severe inflammation were present. Coagulative necrosis of the epidermis without granulation tissue was noted in the untreated groups. After 28 days, there were no differences between the groups in tensile strength, maximum stress, yield strength and stiffness. | [65] |
Gundelia tournefortii aerial parts unspecified extract | Wistar albino rats, male | Second-degree thermal burn—metal plate heated in a flame for 5 min, applied for 8 s | Once a day for 21 days E: extract with milk-cream (4:1) S: 1% SSD cream NC: w/o treatment | From day 7, the wound dimensions of the experimental group and the standard were significantly smaller than those of the controls. From day 14, significantly greater wound closure was observed in the experimental group than in the other groups. After 21 days, the histopathological analysis in the experimental group showed a reduction in inflammation and an increase in the degree of re-epithelialisation and the length of blood vessels compared to the standard group. In addition, there was a significantly higher total volume of collagen fibres, and the scab covered a larger wound area than in the control group. | [66] |
Hippophaë rhamnoides leaves aqueous extract | Sprague-Dawley rats, male | Third-degree thermal burn—metal rod heated to 85 °C, applied for 20 s | Twice a day for 7 days E: 2.5, 5, 7.5 or 10% of extract in soft white petroleum S: 1% SSD cream C: soft white petroleum | The wound area on days 4 and 8 was the smallest in the group treated with 5% extract. Also in this group, significantly higher contents of hydroxyproline, hexosamine, protein, matrix metalloproteinase 9, vascular endothelial growth factor, type-III collagen, and antioxidants (glutathione, vitamin c, superoxide dismutase, catalase, glutathione S-transferase and malondialdehyde) were found in the granulation tissue than in control. The epidermis thickness in this group was comparable to the standard group and significantly higher than in the control group, and the density of blood vessels was significantly higher than in the other groups. | [67] |
Hippophaë rhamnoides seeds oil | Merino sheep, female | Third-degree flame burns—applied with a Bunsen gas burner | Every 6 days for 18 days E: 20 mL of oil C: w/o treatment | The re-epithelialisation time was significantly shortened in the treated group, and the degree of epithelialisation was significantly higher than in the control group. There were no statistically significant differences between the groups in the mean peripheral blood flow and the mean content of malondialdehyde and superoxide dismutase in the wound. | [68] |
Hippophaë rhamnoides leaves aqueous extract | Sprague-Dawley rats, male | Third-degree thermal burn—metal probe heated to 85 °C, applied for 20 s | Twice a day for 7 days E: 2.5% of extract in soft white petroleum S: 1% SSD cream C: soft white petroleum | In the macroscopic evaluation, the experimental group showed the best wound repair and improvement of the peri-wound skin condition. Compared to the control, the wound of the experimental group had a significantly reduced level of reactive oxygen species and the inflammatory response (3-nitrotyrosinase, nitric oxide synthase-2, tumour necrosis factor α, interleukin 1β, interleukin 6 and NF-κB), as well as significantly increased expression of markers responsible for cell proliferation, epithelial migration, angiogenesis, skin hydration, and cytoprotection (proliferating cell nuclear antigen, cytokeratin-14, cluster of differentiation 31, aquaporin 3, hypoxia-inducible factor 1α, glucose-regulated protein 78, and transient receptor potential vanilloid 3). In contrast to the control and standard groups in the treated group, the tissue was characterised by a well-organised orientation with increased mature collagen and rapid epithelial migration towards the wound bed. Increased activity of hexokinase, citrate synthase, glucose-6-phosphate dehydrogenase, mitochondrial enzyme cytochrome c oxidase and an increase in adenosine triphosphate levels were noted, and lower activity of lactate dehydrogenase. | [69] |
Hypericum perforatum seeds oil | Sprague-Dawley rats, male | Second-degree thermal burn—iron plate heated in boiling water for 5 min, applied for 20 s | Once a day for 20 days E: 2 mL of oil NC: w/o treatment | In the treatment group, re-epithelialisation was complete after 21 days, while in the control group, no epidermal layer was formed. In the histopathological analysis of the experimental group, significantly fewer inflammatory cells and increased angiogenesis were observed than in the control group. | [70] |
Juglans regia seeds grounded into ointment | Guangxi Bama mini-pigs, female | Third-degree thermal burn—aluminium plate heated in boiling water for 10 min, applied for 45 s. The wounds were left unhealed for 3 weeks. | After 3 weeks, the wound was cleaned and treated twice daily for 28 days. E: walnut ointment S: recombinant human Epidermal Growth Factor C: normal saline | Compared to the control group, the experimental and standard groups showed a significant reduction in the wound area and improved healing from day 7 to day 28. The total wound closure time was 18.44 ± 3.09, 23.56 ± 4.85 and 32.56 ± 5.36 days in the experimental, standard and control groups, respectively. After 28 days, the histopathological analysis showed significantly thinner proliferative and differentiating epidermis layers in the experimental group. The positive staining of P63 (epidermal proliferation marker) and CK10 (epidermal differentiation marker Cytokeratin 10) was stronger in the standard group compared to the others, but in the experimental group, the positive staining of P63 was stronger than in control. | [29] |
Linum usitatissimum seeds oil | New Zealand rabbits, male | Second-degree thermal burn—stainless steel cylinder heated in boiling water for 3 min, applied for 15 s | Once a day (1 g per wound) for 28 days E: linseed oil S: Cicatryl-bio® ointment (sodium hyaluronate + allantoin) C: Vaseline NC: w/o treatment | The degree of wound closure was significantly higher in the experimental and standard groups from day 16 than in the other groups. The total wound healing time was 26 ± 5.8, 32.5 ± 2.8, 35.6 ± 3.9 and 35 ± 1.1 days for the experimental, standard, control, and negative control group, respectively. In the histopathological analysis of the experimental group, compared to the other groups, a smaller number of inflammatory cells, complete re-epithelialisation, reduced thickness and fibrosis of the epidermis, and an increase in the number of capillaries, collagen fibres, fibroblasts, and myofibroblasts were observed. | [71] |
Lobelia alsinoides whole plant ethanolic extract | Wistar albino rats, male | Third-degree thermal burn—metal plate, heated red hot, applied for 30 s | Once a day for 16 days E: 5% or 10% of extract in a simple ointment S: 1% SSD cream C: simple ointment NC: w/o treatment | In the group treated with 10% of the extract, complete macroscopic re-epithelialisation was visible after 12 days, and in the group treated with 5% of the extract after 16 days. In the other groups, after 16 days, the wound was still open and red. In the histopathological analysis after 16 days, the experimental groups, compared to the others, showed neovascularisation, complete re-epithelialisation, fibroblast proliferation, neutrophil infiltration, angiogenesis, increased amount of collagen and decreased inflammation. | [72] |
Malva sylvestris flowers 70% (v/v) ethanolic extract | Albino rats, male | Second-degree thermal burn—metal plate heated in boiling water for 5 min, applied for 10 s | Once a day for 35 days E: 5% or 10% of extract in base cream S: 1% SSD cream C: base cream NC: normal saline | There was a significant increase in the percentage of wound closure in the experimental groups from the 7th day. After 8 days, in the experimental groups, an increase in the thickness of the epidermis and granulation tissue was observed, and the organisation of squamous cell maturation and orthokeratin improved. In addition, after 21 days, a higher degree of scar formation, collagen organisation, formation of hair follicles and lymphatic vessels, and the degree of innervation was observed in the experimental groups. | [73] |
Michelia champaca flowers ethanolic extract | Wistar albino rats, male | Second-degree thermal burn—hot molten wax (80 °C), applied for 8 min | Once a day until healed E: 10% of extract in an ointment base S: 1% SSD cream | The epithelisation period in the experimental group was 18.33 ± 2.42 days and was shorter than in the standard group, which was 21.67 ± 3.01 days. | [74] |
Musa paradisiaca stems methanolic extract | Wistar albino rats | Third-degree thermal burn—red hot steel rod | Once a day for 14 days E: methanolic extract (unspecified concentration and preparation) C: Vaseline | Compared to the control group, the experimental group showed an increase in wound closure percentage, epithelisation, and faster tissue regeneration. | [75] |
Myrtus communis leaves ethanolic extract | Wistar albino rats | Third-degree thermal burn—exposed to 90 °C water bath for 10 s | Twice a day for 48 h E: 5% (w/w) of extract in simple ointment (0.5 g) NC: w/o treatment | In the skin affected by a burn injury, an increase in superoxide dismutase and catalase activity was observed, as was an increase in malondialdehyde and a decrease in glutathione and nitric oxide levels. After the topical application of 5% ointment, a significant reduction in malondialdehyde level, an increase in nitric oxide level, and an increase in superoxide dismutase and catalase were observed. There was no effect on glutathione level and total tissue protein. | [76] |
Nigella sativa seeds oil | Wistar albino rats, male | Second-degree thermal burn—brass probe heated in boiling water, applied for 20 s | Twice a day for 14 days E: 50% of oil + 50% of cold cream S: 1% SSD cream C: cold cream | The experimental and standard groups observed a reduction in the clinical signs of inflammation, such as warmth, redness, and swelling. The histopathological analysis showed a significant increase in granulation tissue thickness in these groups. After 14 days, the wound appearance of the experimental group was the most normal. | [77] |
Olea europaea seeds oil | domestic pigs, female | Second-degree thermal burn—aluminium bar preheated to 400 °C, applied for 20 s, the necrotic epidermis was removed using bromelain-derived agent, Debridase® | Once a day for 14 days E: purified olive oil S: 1% SSD cream NC: w/o treatment | After 14 days, it was observed that treatment efficiency was significantly better in the standard group. There were no significant differences in wound healing between the experimental and no-treatment groups. | [78] |
Olea europaea leaves 70% (v/v) ethanolic extract | Wistar albino rats, male | Third-degree thermal burn—metal plate, heated in 94 °C water for 20 min, applied for 30 s | Twice a day for 21 days E: 10% of extract in Eucerin S: 1% SSD cream NC: w/o treatment | In the macroscopic evaluation from day 14, it was observed that the treated groups had significantly less wound area than the untreated group. Moreover, the wound area of the experimental group was significantly smaller than that of the standard group. In the histopathological evaluation after 14 days, it was observed that the number of neutrophils and macrophages in the wound significantly decreased in the treatment groups, and the number of fibroblasts increased. There were no differences between the groups in the number of endothelial cells. | [79] |
Onosma dichroanthum roots acetone extract | Wistar albino rats, female | Second-degree thermal burn—metal rod heated in boiling water to 95 °C, applied for 10 s | Once a day for 14 days E: 2% of extract in a base ointment S: 1% SSD cream C: base ointment NC: w/o treatment | After 14 days in the standard group, 2 rats had the wound completely healed, and in the remaining rats, the area was significantly reduced compared to the control groups. On the other hand, in the experimental group, the surface area not only did not decrease but increased its surface area. | [80] |
Onosma bulbotrichum roots n-hexane and dichloromethane (1:1) extract | rabbits, either sex | Second-degree thermal burn—steel plate heated to 150 °C, applied for 20 s | Twice a day until healed E: 1, 2 or 5% of extract in cold cream S: 1% SSD cream C: cold cream NC: w/o treatment | In the study, it was observed that in the standard group and the group treated with 5% of the extract, the time to complete wound healing was significantly shortened to 16 and 17 days, respectively. In contrast, in the control group and the negative control, it was 24 and 26 days, respectively. Compared to the control groups, the wounds of the treatment groups had a significantly higher content of collagen and non-collagen proteins. The histopathological analysis observed the best wound healing in the group treated with the ointment with 5% extract. | [81] |
Phyllanthus niruri whole plant ethanolic extract | Wistar albino rats, male | Second-degree thermal burn—hot wax (80 °C), applied for 8 min | Once a day until healed E: 10% of extract in a simple ointment S: 1% SSD cream | Compared to the group treated with 1% silver sulfadiazine cream, topical administration of an emulgel containing 10% of the extract does not reduce the wound area or shorten the epithelisation period. | [82] |
Pistacia atlantica resin hydrodistillation | Wistar albino rats, female | Third-degree thermal burn—aluminium plate heated to 100 °C, applied for 10 s | Once a day for 14 days E: 5, 10 or 20% of resin oil in the ointment base C: ointment base | There were no significant differences in the size of the wound in the study groups in the macroscopic assessment. In the microscopic and histopathological evaluation, the groups treated with the emulgel with 5 or 10% of the extract developed more capillaries, and significantly higher concentrations of basic fibroblast growth factor and platelet-derived growth factor were observed than in the control group. | [83] |
Pistacia atlantica mastic gum ethanolic extract and essential oil | albino rabbits, male | Second-degree thermal burn—metal plate | Once a day for 21 days E: 30% (9.12 mL of extract + 24.15 mL of essential oil) or 60% (18.24 mL of extract + 48.3 mL of essential oil) of composition in Eucerin C: 30 or 60% of distilled water in Eucerin | After 21 days, the degree of wound closure was significantly higher and amounted to 65% and 94%, respectively, for the group treated with 30% and 60% of the extract, and for the corresponding control groups, 8% and 10%, respectively. Blood concentrations of glutathione peroxidase, superoxide dismutase, catalase, and HDL in the treatment groups were significantly elevated compared to controls. Contrary to control groups, glucose concentration was not elevated. However, there were no significant differences between the groups in malondialdehyde and LDL concentrations. | [84] |
Pistacia atlantica resin oil purchased | Sprague-Dawley rats, male | Third-degree thermal burn—aluminium plate heated to 100 °C, applied for 15–20 s | Once a day (200 mg/kg body weight) for 14 days E: resin oil S: 1% SSD cream NC: w/o treatment | The degree of wound closure in the experimental group after 14 days was 98.6 ± 2.5% and was comparable to the standard group (94.7 ± 4.1%) and significantly higher than in the negative control group (71.2 ± 3.4%). The level of superoxide dismutase, glutathione peroxidase, total antioxidant status, vascular endothelial growth factor, and hydroxyproline was significantly higher in the experimental group compared to the negative control group and the standard group. The malondialdehyde level was comparable to the standard group and higher than the control group. | [85] |
Pistacia lentiscus oil cold pressed | New Zealand rabbits, male | Third-degree thermal burn—metal cylinder heated for 3 min in boiling water, applied for 15 s | Once a day until healed E: 1 mL of oil S: 1% Madecassol® (with Centella asiatica) C: Vaseline NC: w/o treatment | The period of complete re-epithelisation in the treatment groups was 30 ± 3.94 and 33.5 ± 3.78 days in the experimental and standard groups, respectively. It was significantly shorter than in the negative control group, which was 37.16 ± 3.54 days, but it was not considerably different from the group receiving Vaseline (34.66 ± 3.88 days). | [86] |
Plantago major seeds aqueous extract | Sprague-Dawley rats, male | Third-degree thermal burn—hot metal plate | Once a day for 21 days E: 20 or 50% of extract in Eucerin S: 1% SSD cream C: Eucerin | There were no statistically significant differences between the groups in wound size. However, in the histopathological analysis of the wound in the experimental group, in contrast to the control group, good re-epithelialisation and organisation of the granulation tissue were observed. Parallel-oriented fibroblasts were present in the well-structured layer of the epidermis, and the number of inflammatory cells and capillaries was high. | [87] |
Pothos scandens leaves ethanolic extract | Wistar albino rats, either sex | Thermal burn—iron plate heated in a flame to red hot, applied for 10 s | Once a day for 20 days E: 2, 4, 6, 8 or 10% of extract in glycerol C: glycerol NC: w/o treatment | The extract’s application significantly reduced the re-epithelialisation time compared to the control groups. The shortest time was obtained in the group treated with 4% extract (22 ± 2.43 days). In the control group, the time was 35 ± 1.69 days, and in the negative control group, 40 ± 1.06 days. | [88] |
Punica granatum peel standardised pomegranate rind extract (13% of ellagic acid) | Wistar albino rats, male | Third-degree thermal burn—metal rod heated to 100 °C in boiling water, applied for 20 s | Once a day (0.5 g per wound) for 12 days E: 1, 2.5 or 5% of extract in formulation base S: 1% SSD cream C: formulation base | Significant differences in the percentage of wound closure between the treatment and control groups were observed from day 4 onwards. The extract reduced the wound surface area in a concentration-dependent manner and was comparable to 1% silver sulfadiazine cream. In addition, in the standard group and, depending on the concentration, in the experimental groups, a significant reduction in myeloperoxidase activity was observed, which is an indicator of inflammatory neutrophil infiltration. | [89] |
Punica granatum fruits standardised pomegranate extract (40% of ellagic acid) | albino rats (Rattus norvegicus), male | Second-degree thermal burn—steel plate heated to 85 °C, applied for 5 s | Twice a day for 14 day E: 2.5, 5 or 10% of extract in a cream base S: 1% SSD cream C: cream base | The experimental groups showed higher re-epithelialisation and collagen levels and reduced neutrophil infiltration and angiogenesis than the control and standard groups. | [90] |
Punica granatum fruits methanolic extract | minipigs, either sex | Second-degree thermal burn—fuel smeared on the skin and lit by an open fire for 45 s | Twice a day for 28 days E: 5% of extract in base gel S: 1% SSD cream or 20 g/kg Jing Wan Hong herbal ointment C: base gel NC: w/o treatment | After 28 days of treatment, the skin morphology in the experimental group improved and was close to normal skin. Compared to the control, comparable acceleration of healing, shortening of healing time, and elimination of scab and fur growth were observed in the experimental and standard groups. From day 7, the treatment groups showed an increase in vascular endothelial growth factor A and transforming growth factor β1 levels compared to the control groups. | [91] |
Rubus caesius leaves 70% (v/v) ethanolic extract | Wistar albino rats, male | Third-degree thermal burn—steel device heated in boiling water (100 °C), applied for 5 s | Once a day for 21 days E: 10% of extract in cold cream S: 1% SSD cream C: cold cream | After 7 days, compared to the control and standard group, a higher number of capillaries was observed in the experimental group, and their number decreased in the following days. After 21 days, an almost complete wound healing with well-rebuilt granulation tissue and no inflammatory cells were observed in the experimental group and incomplete epithelisation and infiltration of inflammatory cells in the control and standard groups. | [92] |
Sambucus nigra flowers, leaves 70% (v/v) ethanolic extract | Wistar albino rats, male | Third-degree thermal burn—steel device heated in boiling water (100 °C), applied for 5 s | Once a day for 21 days E: 10% of extract of flowers or leaves in cold cream S: 1% SSD cream C: cold cream | Compared to the control group and the standard, the experimental group had a higher number of capillaries after 7 days, and their number decreased in the following days. After 21 days, an almost complete wound healing with well-rebuilt granulation tissue and no inflammatory cells were observed in the experimental group and incomplete epithelisation and infiltration of inflammatory cells in the control and standard groups. | [92] |
Sauromattum guttatum tubers 70% (v/v) methanolic extract | BALB/c mice, either sex | Second-degree thermal burn—metal bar heated on opened flame, applied for 9 s | Three times a day for 15 days E: 2% of extract in petroleum jelly S: 1% SSD cream C: petroleum jelly NC: w/o treatment | After 15 days, the experimental and standard groups showed a reduction in wound area compared to the control group. In the histopathological analysis, in the treated groups, in contrast to the control groups, a normal healing process was observed, i.e., normal regeneration of the epidermis, the presence of new capillaries, granulation tissue, sebaceous glands and hair follicles. In addition, the treatment groups increased the expression of platelet-derived growth factor, epidermal and fibroblast growth factor. | [93] |
Sanguisorba officinalis roots 70% (v/v) ethanolic extract | Sprague-Dawley rats, male | Second-degree thermal burn—electrical scald instrument (75 °C), applied for 15 s | Twice a day for 14 days E: 1 mL of extract (100 mg/mL) S: 0.3 g of 1% SSD cream NC: w/o treatment | After 14 days, the experimental and standard groups’ wounds was significantly smaller than the wound of the control group. In the histopathological analysis in the treatment groups, rapid progression of reepithelialisation, formation of granulation tissue, collagen fibres and blood vessels, and disappearance of inflammatory cells were observed in contrast to the negative control. | [94] |
Senna podocarpa leaves 50% (v/v) ethanolic extract | Wistar albino mice, either sex | Second-degree chemical burn—hydrochloric acid (0.2 mL, 37%), applied for 15 s | Once a day for 14 days E: 2.5 or 7.5% of extract in base emulgel or extract poultice S: 1% SSD cream C: base emulgel NC: w/o treatment | The degree of wound closure after 14 days was 64, 87, 50 and 66% for the group treated with 2.5% extract, 7.5% extract, extract poultice and 1% SSD cream, respectively. In contrast, in the control groups, the degree of wound closure was below 10%. The group treated with 7.5% extract in emulgel had the best results in histopathological analysis, with significantly higher levels of keratin, epidermal cells, gland cells, adipocytes, and collagen than in the control and standard groups. However, more inflammatory cells and fewer elastin fibres were also observed. | [95] |
Sesamum indicum oil cold pressed | BALB/c albino mice, male | Third-degree thermal burn—coin heated for 3 min with a spirit lamp, applied for 8 s | Once a day for 28 days E: 30 or 40% of oil NC: w/o treatment | Compared to the negative control, the group treated with sesame oil showed better wound healing. The level of total antioxidant power was significantly higher, and the level of malondialdehyde significantly lower than in control. | [62] |
Terminalia chebula fruits 70% (v/v) ethanolic extract | Wistar albino rats, male | Second-degree thermal burn—hot water (90 °C), applied for 6 s | Once a day for 30 days E: 5 or 10% of extract in base cream S: 1% SSD cream C: base cream NC: normal saline | The wound size decreased the most in the group treated with the cream with 10% extract. Significant differences in wound size between this group and the other groups were evident from day 10. Complete wound closure was seen after 20 days in the 10% extract cream group, 25 days in the 5% extract cream group, and 33–35 days in the standard and control groups. In the morphological and histopathological analysis, inflammatory cell infiltration, neovascularisation, fibroblast proliferation, mucopolysaccharide deposition in the matrix, degree of inflammation, the extent of bacterial colonisation, and degree of granulation tissue formation were scored. Statistically, the best results, indicating an advanced degree of healing, were obtained for the group treated with cream with 10% of the extract. The group treated with the cream with 5% extract obtained as good results as the standard group. | [96] |
Tragopogon graminifolius aerial parts 80% (v/v) ethanolic extract | Wistar albino rats, male | Second-degree thermal burn—aluminium rod, heated to 110 °C, applied for 10 s | Once a day for 14 days E: 5 or 10% of extract in Eucerin S: 1% SSD cream C: Eucerin | After 14 days, the wound area was reduced by 80, 73, 78, and 58% in the 10% extract, 5% extract, standard, and control groups, respectively. Significant differences were observed in the standard group and the group treated with 10% extract compared to the control. In these two groups, also in the histopathological analysis, re-epithelialisation of the epidermis and a significantly better profile of biomarkers of tissue oxidative stress, including a higher content of total thiol molecules and lower lipid peroxidation, were visible. The control and experimental groups observed no differences in total antioxidant power. | [97] |
Tridax procumbens leaves 90% (v/v) ethanolic extract | Wistar albino rats, male | Second-degree thermal burn—hot wax (80 °C), applied until solidified | Once a day (0.5 g per wound) for 15 days E: 1% of extract in base gel S: 1% SSD cream C: base gel | Wound closure after 15 days was 69.14 ± 0.7497% in the experimental group, 90.43 ± 0.7691 % in the standard group, and 68.58 ± 0.7791% in the control group. The mean re-epithelisation time was 32.10 ± 0.86 days in the experimental group, 25.20 ± 2.10 days in the standard group and 38.36 ± 1.77 days in the control group. There were no statistical comparisons. | [50] |
Viola tricolour flowers 70% (v/v) ethanolic extract | Wistar albino rats, male | Sunburn—UVB radiation: 0.27 mW/cm2, 0.5 J/cm2 | Once a day for 6 days E: 1, 3 or 10% of extract in base gel S: 1% SSD cream C: base gel | In the groups treated with 3 and 10% of the extract, static and dynamic allodynia and paw oedema were significantly reduced, and the increase in myeloperoxidase activity was inhibited compared to the control, showing effectiveness comparable to that in the standard group. | [98] |
Vitis vinifera leaves 30% (v/v) methanolic extract | Wistar albino rats, male | Second-degree thermal burn—metal plate heated in boiling water for 5 min, applied for 10 s | Twice a day for 21 days E: 0.5, 1, 1.5 or 2% of extract in Eucerin S: 1% SSD cream C: Eucerin NC: w/o treatment | Wound healing in the experimental groups was better than in the control groups. Wound healing in the experimental group was worse (for 0.5, 1 and 1.5%) or comparable (for 2%) than in the standard group. The groups treated with 1.5 and 2% of the extract showed better healing parameters than the control groups, such as the number of hair follicles, sebaceous glands, fibroblasts, macrophages, neutrophils, blood vessels, and the thickness of the epidermal layer. | [47] |
Zanthoxylum bungeanum seeds oil (expeller pressed) | Sprague-Dawley rats, male | Second-degree thermal burn—hot water (100 °C), applied for 12 s | Twice a day for 7 days, then once a day until healed E: 0.5 or 1 mL of oil per wound S: 1% SSD cream NC: w/o treatment | From day 7 of treatment, a dose-dependent increase in wound healing was observed in the experimental groups compared to the controls. The increase for the group treated with 1000 µL of oil was comparable to the standard group. Histopathological analysis showed a statistically significantly thicker epidermal layer in the treated groups compared to the controls, but no significant differences in skin thickness were found. Levels of superoxide dismutase, hydroxyproline, and type-III collagen were significantly higher in experimental and standard groups compared to controls. However, the level of malondialdehyde, matrix metalloproteinase 2, matrix metalloproteinase 9, tumour necrosis factor α, interleukin 6, interleukin 1β, phosphor-nuclear factor-κB p65, and phosphor-inhibitor of nuclear factor-κB subunit α was significantly lower in these groups compared to controls. | [99] |
Composition of the Mixture | Animal Model | Burn Wound | Treatment Schedule * | Results | Ref. |
---|---|---|---|---|---|
Allium sativum (bulbs; squeezed juice)Euphorbia honey | Wistar albino rats, either sex | Thermal burn—metal plate, heated in boiling water for 10 min, applied for 20 s | Once a day until healed E: Euphorbia honey or a mixture of Euphorbia honey and Allium sativum juice (amount and concentration not given) S: Betadine solution or 1% SSD cream | The shortest time needed for complete epithelisation and wound closure was noted for the group treated with the mixture, 1% SSD cream, and then for the group treated with Euphorbia honey. The longest time was recorded in the group treated with betadine. In the histological examination, the group treated with the mixture was characterised by a thicker layer of epidermis and skin than the other groups. There were no differences between the groups in the interdigitation index and the orientation of collagen fibres. | [100] |
Aloe vera leaves Vitis vinifera leaves 30% (v/v) methanolic extracts | Wistar albino rats, male | Second-degree thermal burn—metal plate heated in boiling water for 5 min, applied for 10 s | Twice a day for 21 days E: the combination of leaf extracts in a ratio of 1.5%:1.5% in Eucerin S: 1% SSD cream C: Eucerin NC: w/o treatment | The wound area of the experimental group after 7, 14 and 21 days was significantly smaller than the wounds of the control groups but comparable to the standard group. It has been observed that treatment with the composition has better healing effects than treatment with the individual components. Compared to the control and standard groups, the experimental group showed a higher degree of tissue maturation and organisation and re-epithelialisation, a fully formed epidermis, more hair follicles, sebaceous glands, fibroblasts and capillaries, and a decrease in neutrophil and macrophage infiltration. | [47] |
Arctocarpus heterophyllus, fruits Murraya koenigii leaves Nerium indicum, leaves Punica granatum, bark 70% (v/v) ethanolic extracts | albino rats, either sex | Third-degree chemical burn—sulphuric acid, applied for 10 s | Once a day until healed E: 10% or 15% of the combination of extracts (1:1:1:1) in ointment base or base gel S: Povidone-iodine C: ointment base or base gel NC: w/o treatment | The period of epithelialisation in the experimental groups with the basic ointment, the basic gel, and the standard group was significantly shorter than in the corresponding control groups. In addition, it was shorter than in the groups treated with single components. Hydroxyproline level and tensile strength were higher in the experimental and standard groups than in the controls. In the histopathological analysis, better wound healing parameters were observed in the experimental groups with base ointment than with base gel. | [101] |
Azadirachta indica leaves Tridax procumbens leaves Honey 90% (v/v) ethanolic leaf extracts | Wistar albino rats, male | Second-degree thermal burn—hot molten wax (80 °C), applied until solidified | Once a day for 15 days E: herbal gel (unspecified concentration) S: 1% SSD cream C: base gel | The degree of wound closure after 15 days was 89.35 ± 0.4155, 90.43 ± 0.7691 and 68.58 ± 0.7791%, and the period of epithelisation was 26.32 ± 2.22, 25.20 ± 2.10 and 38.36 ± 1.77 days in the experimental, standard and control groups, respectively. The results obtained in the experimental group were as good as in the standard group and significantly better than in the control group. Moreover, the formulation has been shown to have synergistic activity in wound healing as the results obtained are better than those of the single components of the formulation. | [50] |
Calendula officinalis Rosa damascena Beeswax | Wistar albino rats, male | Second and third-degree thermal burn—metal plate heated in boiling water for 5 min, applied for 10 or 30 s | Once a day for 40 days E: commercial herbal ointment Robacin® (the exact composition is not given) S: 1% SSD cream or Aloe vera cream | In the second-degree burn group treated with herbal ointment, wound healing was significantly fastest for the first two weeks and comparable to the standard groups. In the third-degree burn group, wound closure was the fastest in the experimental group. In both burns (second and third degree), a much smaller extent of angiogenesis and fibrosis was observed in the experimental group than in the standard groups. In third-degree burns, epithelialisation in the experimental group was as good as in the Aloe vera cream treatment. | [102] |
Cannabis sativa Juglans regia Pistacia atlantica Sesamum indicum cold pressed oils | albino mice, male | Third-degree thermal burn—boiling water (100 °C), applied for 10 s | Twice a day for 21 days E: the combination of sesame oil (60%), pistachio oil (20%), hemp oil (12%) and walnut oil (8%) S: 1% SSD cream NC: w/o treatment | The degree of wound closure was 99.5 ± 0.8, 78.0 ± 4.0 and 88.4 ± 2.5% in the experimental, standard and control groups. The differences between the groups were statistically significant. In the experimental, standard and control groups, the time to complete epithelisation was 20.5 ± 1.37, 26.33 ± 0.81 and 25.5 ± 0.83 days. It was significantly shorter in the group treated with the oil composition. | [103] |
Centella asiatica, herb, 70% (v/v) ethanolic extract Papaya latex, dried and powdered | albino mice, male | Chemical burn—50% phenol solution, applied for 30 s | Once a day for 10 days E: C. asiatica and papaya latex in a ratio of 1%:1%, 0.5%:1.5% and 1.5%:0.5% in a base gel S: Bioplacenton® jelly (neomycin + placenta extract) C: base gel | Complete wound closure was achieved after 6 days in the experimental group in the ratio of 1:1 and in the standard group. After 7 days, it was achieved in the groups in the ratio of 1.5:0.5 and 0.5:1.5. After 10 days, in the control group, the wound closure was only 75.34 ± 20.709%. The combination of C. asiatica and papaya latex showed a synergistic effect on wound healing, as in the case of the components used alone. Complete wound closure was observed after 8 days. | [56] |
Cucurbita moschata Sesamum indicum oils | BALB/c albino mice, male | Third-degree thermal burn—coin heated for 3 min with a spirit lamp, applied for 8 s | Once a day for 28 days E: the combination of oils (1:1) NC: w/o treatment | In the experimental groups, wound healing was significantly better than in the negative control and the groups treated separately with sesame oil and pumpkin oil. In addition, a significantly higher level of total antioxidant power and a lower level of malondialdehyde were obtained than in the other groups. | [62] |
Malva sylvestris, leaves, aqueous extract Rosa damascena, petal powder, sesame oil extract Solanum nigrum, leaves, aqueous extract | Wistar albino rats, male | Second-degree thermal burn—electrical heater heated to 110 °C, applied for 10 s | Once a day for 14 days E: herbal ointment (5% of each aqueous extract and 33% of oily extract in base ointment) S: 1% SSD cream C: base ointment NC: without treatment | After 14 days of treatment, the wound closure was the highest in the group treated with herbal ointment and amounted to 87.0 ± 2.1%. The remaining groups were 70.8 ± 3.5, 57.0 ± 5.3 and 32.2 ± 1.6% in the standard, control, and negative control groups. Compared to the other groups, the histopathological analysis in the experimental group showed a significant improvement in wound healing with complete re-epithelialisation, well-formed granulation tissue and mild infiltration of inflammatory cells. In addition, advanced neovascularisation, and irregular distribution of myofibroblasts, fibroblasts and collagen fibres were present. | [104] |
Momordica charantia, fruits Piper nigrum, fruits Pongamia glabra, leaves aqueous extracts | albino rats, either sex | Third-degree chemical burn—sulphuric acid, applied for 10 s | Once a day for 21 days E: 10% or 15% of the combination of extract (1:1:1) in the ointment base S: Povidone-iodine ointment C: ointment base NC: w/o treatment | The period of epithelialisation was 14.97 ± 0.256, 14.77 ± 0.207 and 15.5 ± 0.315 days in the group treated with 10% ointment, 15% ointment and standard, respectively, and was significantly shorter in these groups than in the control groups, where it was 18.18 ± 0.345 and 18.88 ± 0.259 days in the control and negative control groups, respectively. Hydroxyproline levels and tensile strength were significantly higher in experimental and standard groups compared to controls. In the histopathological analysis in the experimental and standard groups, better wound healing, fewer inflammatory cells, a thicker layer of granulation tissue and epidermis, and more dermal fibrosis were observed than in control. | [105] |
Rhododendron macrophyllum Thymus serpyllum | Wistar albino rats, male | Second and third-degree thermal burn—metal plate heated in boiling water for 5 min, applied for 10 or 30 s | Once a day for 40 days E: commercial herbal ointment Rimojen® (the exact composition is not given) S: 1% SSD cream or Aloe vera cream | In both the second and third-degree burn groups, wounds treated with herbal ointment healed much more slowly than those treated with Aloe vera cream and 1% silver sulfadiazine cream. | [102] |
Sesamum indicum oil Camphora Honey | Wistar albino rats, male | Second-degree thermal burn—hot metal plate, applied for 10 s | Once a day for 28 days E: herbal ointment (the exact composition is not given) C: Vaseline | The percentage of wound healing from day 7 was higher for the group treated with herbal ointment than Vaseline. Moreover, neovascularisation was higher in the group treated with herbal ointment than in the control group. | [106] |
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Skowrońska, W.; Bazylko, A. The Potential of Medicinal Plants and Natural Products in the Treatment of Burns and Sunburn—A Review. Pharmaceutics 2023, 15, 633. https://doi.org/10.3390/pharmaceutics15020633
Skowrońska W, Bazylko A. The Potential of Medicinal Plants and Natural Products in the Treatment of Burns and Sunburn—A Review. Pharmaceutics. 2023; 15(2):633. https://doi.org/10.3390/pharmaceutics15020633
Chicago/Turabian StyleSkowrońska, Weronika, and Agnieszka Bazylko. 2023. "The Potential of Medicinal Plants and Natural Products in the Treatment of Burns and Sunburn—A Review" Pharmaceutics 15, no. 2: 633. https://doi.org/10.3390/pharmaceutics15020633
APA StyleSkowrońska, W., & Bazylko, A. (2023). The Potential of Medicinal Plants and Natural Products in the Treatment of Burns and Sunburn—A Review. Pharmaceutics, 15(2), 633. https://doi.org/10.3390/pharmaceutics15020633